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A longitudinal study based on patient-reported outcomes after cervical cancer surgery

A longitudinal study based on patient-reported outcomes after cervical cancer surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113990
Enrollment
Unknown
Registered
2025-12-05
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cervical cancer

Interventions

Reliability and validity verification group:None
longitudinal cohort study group:None

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients who are initially diagnosed with primary cervical cancer and scheduled to undergo surgery.

Exclusion criteria

Exclusion criteria: Patients who are aged < 14 years or have cognitive impairment, nable to complete the scale.

Design outcomes

Primary

MeasureTime frame
Gynecological cancer perioperative symptom scale;—

Secondary

MeasureTime frame
Progression-free survival;Overall survival;Interval of anti-tumor treatment;—

Countries

China

Contacts

Public ContactQu Dacheng

Affiliated Hospital of North Sichuan Medical College

qdc3253859@163.com+86 138 9074 5770

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026